Senior Medical Writer (m/f/d)

It\'s a good feeling to know you\'re doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We are hiring a Senior Medical Writer (m/f/d) – Hechingen, Germany or Remote within EMEA

Your Strength

• At least 4 years of experience in medical writing or a related field
• Advanced degree in a scientific or technical discipline (PhD or MD preferred)
• Solid clinical knowledge, ideally with background in Cardiology
• Proven experience in authoring clinical research documents and regulatory submissions
• Strong ability to independently evaluate and interpret medical literature and data
• In-depth knowledge of medical writing standards, clinical evaluation (e.g. CERs, PMCF), and MDR requirements
• Excellent English communication skills; scientific writing fluency is essential
• Skilled in cross-functional collaboration with departments such as Clinical Affairs, R&D, RA/QA, and Marketing
• Experience mentoring or reviewing work of junior medical writers is a plus

Your Contribution

• Act as lead writer on complex projects (global/multi-project/new product development)
• Write, review, and submit scientific manuscripts, abstracts, presentations, and regulatory documentation
• Author Clinical Evaluation Reports (CERs), PMCF Plans, Clinical Evaluation Plans, and related documents
• Independently conduct gap analysis and evidence assessments
• Evaluate technical file documents (e.g. risk management, IFU) against clinical and literature data
• Collaborate with internal stakeholders (Clinical, R&D, RA, QA, Marketing) and external partners (CROs, surgeons)
• Support response to regulatory authority questions and submissions
• Conduct state-of-the-art evaluations and risk/benefit assessments across the product lifecycle
• Develop and implement literature search strategies and critically assess scientific validity and relevance
• Take ownership of assignments with minimal supervision and contribute as a subject matter expert

Our Strength

• A mission-driven Clinical Affairs team with a focus on innovation and quality
• High-impact role with direct contribution to product safety and compliance
• Structured onboarding and continuous learning opportunities
• Hybrid or remote work flexibility within EMEA
• Attractive benefits including pension plan and EGYM Wellpass

Contact

Apply now and join the Artivion team. We are looking forward to receiving your application documents in English directly via our online system. Brian Russo, T:

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,

Lotzenäcker 23, 72379 Hechingen

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